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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received October 19, 2004
Accepted December 14, 2004
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Adsorption Isotherm of Ibuprofen on Molecular Imprinted Polymer

Center for Advanced Bioseparation Technology and Dept. of Chem. Eng., Inha University, 253 Yonghyun-Dong, Nam-Ku, Incheon 402-751 136-791, Korea
rowkho@inha.ac.kr
Korean Journal of Chemical Engineering, March 2005, 22(2), 264-267(4), 10.1007/BF02701495
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Abstract

A molecular imprinted polymer (MIP) using (+)-(S)-2-(4-isobutylphenyl) propionic acid ((+)-(S)-ibuprofen) as the template and 4-vinylpyridine (4-VPY) as the functional monomer was prepared. Chloroform and acetonitrile were used as the porogen with ethylene glycol dimethacrylate (EGDMA) as the crosslinker and 2,2'-azobis(isobutyronitrile) (AIBN) as the initiator. Comparison of ibuprofen adsorption isotherm on molecular imprinted and blank polymers was made by the static method. The adsorption equilibrium data were correlated into the Freundlich, Langmuir, Sips (Langmuir-Freundlich) and Radke-Prausnitz isotherm models, respectively. By a nonlinear regression analysis, the experimental parameters in the equilibrium isotherms were estimated and compared. The calculated data is well fitted with the experimented data. Through the analysis, the ibuprofen imprinted polymer showed higher adsorption ability than blank polymer.

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